FDA Enforcement Class II Terminated

Multi-Lumen Central Venous Catheterization Kit with Blue FlexTip(R), ARROWg+ard Blue PLUS(R) Catheter and Sharps Safety Features; Product Codes: ASK-42703-MHW and ASK-42703-OLL1

Recall: Z-1987-2018 · Reported June 6, 2018

Enforcement

Recall Number
Z-1987-2018
Event ID
79890
Classification
Class II
Status
Terminated
Product Type
Devices
Firm
Arrow International Inc
Voluntary / Mandated
Voluntary: Firm initiated
Initial Notification
Letter
Report Date
June 6, 2018
Initiation Date
April 11, 2018
Classification Date
May 30, 2018
Termination Date
May 15, 2020
Address
2400 Bernville Rd, N/A, Reading, PA, 19605-9607, United States

Description

Multi-Lumen Central Venous Catheterization Kit with Blue FlexTip(R), ARROWg+ard Blue PLUS(R) Catheter and Sharps Safety Features; Product Codes: ASK-42703-MHW and ASK-42703-OLL1

Reason

Product sterility may be compromised due to unsealed packaging.

Code Info

Lot Numbers: Product Codes ASK-42703-MHW: 13F16M0282 13F17D0183 13F17H0260 13F17M0344 Product Code ASK-42703-OLL1: 13F17C0293 13F17E0414 13F17J0243

Distribution

US Nationwide, AUSTRALIA, AUSTRIA, BELGIUM, CANADA, CZECH REPUBLIC, DENMARK, ECUADOR, FRANCE, GERMANY, GREECE, HONG KONG, INDONESIA, IRELAND, ITALY, JAPAN, KOREA, NETHERLANDS, NEW ZEALAND, PANAMA, PHILIPPINES, POLAND, PUERTO RICO, ROMANIA, SAUDI ARABIA, SINGAPORE, SLOVENIA, SOUTH AFRICA, SPAIN, SWEDEN, SWITZERLAND, THAILAND, TRINIDAD AND TOBAGO, UNITED KINGDOM

Quantity

416,055 total products